Suppr超能文献

抗ICAM-1反义寡脱氧核苷酸对麻醉大鼠肾缺血再灌注损伤的影响。

Effect of antisense oligodeoxynucleotides for ICAM-1 on renal ischaemia-reperfusion injury in the anaesthetised rat.

作者信息

Kiew Lik Voon, Munavvar Abdul Sattar, Law Chung Hiong, Azizan Abdullah Nor, Nazarina Abdul Rahman, Sidik Khalifah, Johns Edward J

机构信息

Department of Pharmaceutical Sciences, University of Science Malaysia, Penang, Malaysia.

出版信息

J Physiol. 2004 Jun 15;557(Pt 3):981-9. doi: 10.1113/jphysiol.2004.061788. Epub 2004 Mar 26.

Abstract

An antisense oligodeoxynucleotide (As-ODN) to the 3' untranslated region of the mRNA sequence expressing the intracellular adhesion molecule-1 (ICAM-1) was employed to determine ICAM-1's role in renal ischaemia-reperfusion injury in the rat. Wistar-Kyoto rats receiving i.v. either lipofectin-As-ODN (As-ODN group), lipofectin-reverse ODN (Rv-ODN group) or lipofectin (ischaemia control group) 8 h prior to study were anaesthetized and subjected to 30 min of renal artery occlusion. Renal haemodynamic and excretory parameters were monitored before and after renal ischaemia. On termination of the study renal tissue was subjected to histological and Western blot analysis. Renal blood flow decreased in the 3 h post-ischaemia period in the ischaemia control and Rv-ODN groups, but was maintained in the As-ODN group. Glomerular filtration rate was depressed initially but gradually increased to 10% above basal levels in the ischaemia control and Rv-ODN groups, but was below basal levels (20%) in the As-ODN group. There was a three- to fourfold increase in sodium and water excretion following ischaemia in the ischaemia control and reverse-ODN groups but not in the As-ODN treated group. The As-ODN ameliorated the histological evidence of ischaemic damage and reduced ICAM-1 protein levels to a greater extent in the medulla than cortex. These observations suggested that in the post-ischaemic period afferent and efferent arteriolar tone was increased with a loss of reabsorptive capacity which was in part due to ICAM-1. The possibility arises that the action of ICAM-1 at vascular and tubular sites in the deeper regions of the kidney contributes to the ischaemia-reperfusion injury.

摘要

采用针对表达细胞间黏附分子 -1(ICAM -1)的mRNA序列3'非翻译区的反义寡脱氧核苷酸(As -ODN),以确定ICAM -1在大鼠肾缺血再灌注损伤中的作用。在研究前8小时经静脉注射脂质体 -As -ODN(As -ODN组)、脂质体 -反义寡核苷酸(Rv -ODN组)或脂质体(缺血对照组)的Wistar -Kyoto大鼠被麻醉,并接受30分钟的肾动脉阻断。在肾缺血前后监测肾血流动力学和排泄参数。研究结束时,对肾组织进行组织学和蛋白质印迹分析。缺血对照组和Rv -ODN组在缺血后3小时肾血流量下降,但As -ODN组血流量得以维持。缺血对照组和Rv -ODN组肾小球滤过率最初降低,但逐渐增加至基础水平以上10%,而As -ODN组则低于基础水平(20%)。缺血对照组和反义寡核苷酸组缺血后钠和水排泄增加了三到四倍,但As -ODN处理组未出现这种情况。As -ODN改善了缺血损伤的组织学证据,并在髓质中比皮质更大程度地降低了ICAM -1蛋白水平。这些观察结果表明,在缺血后时期,入球和出球小动脉张力增加,重吸收能力丧失,部分原因是ICAM -1。有可能ICAM -1在肾深部区域的血管和肾小管部位的作用促成了缺血再灌注损伤。

相似文献

8
Prospects of antisense oligodeoxynucleotides to alleviate renal ischaemia-reperfusion injury.
Expert Opin Biol Ther. 2004 Dec;4(12):1931-7. doi: 10.1517/14712598.4.12.1931.

引用本文的文献

7
Sticky wickets in lower nephron nephrosis.下肾单位肾病中的棘手问题。
J Physiol. 2004 Jun 15;557(Pt 3):703. doi: 10.1113/jphysiol.2004.065086. Epub 2004 Apr 8.

本文引用的文献

1
A method for determination of inulin in plasma and urine.一种测定血浆和尿液中菊粉的方法。
Acta Med Scand Suppl. 1952;266:275-82. doi: 10.1111/j.0954-6820.1952.tb13376.x.
5
Biology of acute renal failure: therapeutic implications.
Kidney Int. 1997 Oct;52(4):1102-15. doi: 10.1038/ki.1997.435.
7
Renal ischaemia--reperfusion injury.
Br J Surg. 1996 Feb;83(2):162-70.
8
Mechanisms of ischemic acute renal failure.缺血性急性肾衰竭的机制。
Kidney Int. 1993 May;43(5):1160-78. doi: 10.1038/ki.1993.163.
10
Macrophages in acute glomerular inflammation.
Kidney Int. 1994 Apr;45(4):945-52. doi: 10.1038/ki.1994.128.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验